None listed
Conditions
Interventions
A double blind randomised trial comparing intravenous heparin versus placebo (5% glucose). The infusion will be commenced 8 - 10 hours prior to commencement of surgery and ceased prior to the insertion of lines or sternotomy.
Sponsors
Nil
Study design
Allocation
Randomised controlled trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Adult patients undergong elective cardiac surgery for coronary artery bypass grafting with cardiopulmonary bypass.
Exclusion criteria
Previous adverse reaction to heparin. Active bleeding. An additional surgical procedure to coronary artery bypass grafting planned. Creatinine >200umol/L.
Outcome results
None listed